Infantile Cerebellar-Retinal Degeneration (ICRD)

Sponsored diagnostic testing programs for Infantile Cerebellar-Retinal Degeneration (ICRD)

Infantile cerebellar-retinal degeneration is a severe neurodegenerative disorder characterized by early-onset retinal dystrophy, progressive cerebellar atrophy, hypotonia, and developmental delay. Affected children often develop profound visual impairment and motor disability. Genetic testing confirms the diagnosis and supports counseling and care planning.

1 program found for Infantile Cerebellar-Retinal Degeneration (ICRD)

Programs

1 program
Invitae Unlock™

Invitae Inherited Retinal Disorders Panel

This program offers U.S. clinicians access to comprehensive genetic testing for patients with suspected inherited retinal diseases, including RP, CRD, LCA, Stargardt disease, and other IRDs. Testing is also appropriate for asymptomatic individuals with a family history of IRD or a known pathogenic variant in a relevant gene, supporting diagnosis, risk assessment, and patient management.

Ophthalmology
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